在电化学储能器件中,电极材料是必不可少的组成部分之一。通过巧妙的设计和构建电极材料,可实现储能性能的大幅度提高。那么如何做呢?通过阅读今天这篇综述,或许会给你一些启示!
电极材料
Searching for electrode materials with high electrochemical reactivity
寻找具有高电化学活性的电极材料
Authors: Kunfeng Chen, Dongfeng Xue
Volume 1, Issue 3, Pages 170-187
The most key materials in electrochemical energy storage devices are electrode materials mainly including inorganic cathode and anode materials.
电化学储能器件中最重要的材料是电极,主要包括了无机正极和负极材料。
However, inorganic electroactive materials often suffer from low conductivity, low capacity, low cycling life.
然而,无机电活性材料的导电率、容量和循环寿命都较差。
In order to solve these problems, much research work focused on the design of electrode materials and the construction of novel electrode structures in the field of electrochemical energy storage.
为了解决上述问题,在电化学储能领域中,许多研究工作关注于设计电极材料和构建新型电极结构。
In this review, we reported the latest development of the design principles of the high-performance electrodes for lithium ion batteries and supercapacitors.
在本综述中,报道了锂离子电池和超级电容器的高性能电极的设计原理研究进展。
We mainly discussed three kinds of examples, blended electrode, integrated electrode and in-situ formed electrode, to display the principles of electrode materials design and electrode construction.
以三种电极为例进行了讨论,分别是混合电极(锰基、铜基、铁基)、集成电极(石墨烯纸电极、铜基)和原位形成电极(胶体电极),介绍了电极材料设计和电极构建的原理。
关于电极材料的未来发展之路,作者这样认为:
The new-developed integrated electrode and in-situ formed electrode maybe the promising candidates for next-generation high-performance energy storage devices.
新开发的集成电极和原位形成电极有望用于下一代高性能储能器件。
The finding of the exact physical and chemical process of charge storage mechanism is still challenging.
了解电荷存储机制的确切物理和化学过程仍然是一项具有挑战性的工作。
The new optimized electrode structures are urgent to obtain fast electron transfer rate and the maximization ratio of active materials in electrode.
急需新的优化电极结构的方法以获得快速的电子传输率和最大活性材料比。
For the scale practical application of energy storage devices, the scalable fabrication and the cost of electrode materials are also need to take into account.
为了储能器件的大规模商业化应用,需要开发可量产的制备方法和降低电极材料的费用。
文中部分图片:
Mn基混合电极
Fig. 2. Electrochemical performances of MnO2 anodes obtained by microwave−hydrothermal synthesis. Voltage profiles (a–d) and cycling retention (e,f) of MnO2 were measured as Li-ion battery anode materials at a rate of 100 mA g−1 between 0.01 and 3.0 V. Insets show crystallographic structures of β- and γ- MnO2.
石墨烯纸电极的电化学性能
Fig. 7. Electrochemical characterizations of graphene paper as a lithium-ion battery anode (a and b) and a supercapacitor electrode (c–e). (a) Discharge–charge curves at a current density of 100 mA g−1. (b) Cycle performance at different current densities. (c) CV curves of the graphene paper as a supercapacitor electrode at different scan rates. (d) Specific capacitance of the graphene paper as a function of charge–discharge rate. (e) Cycling test at a current density of 20 A g−1 up to 5000 cycles.
石墨烯纸电极的储能原理
Fig. 8. Charge storage mechanisms of the graphene paper electrode in the traditional electrolyte system (a) and the redox-electrolyte system (b). (a) Graphene paper electrode in the neutral Na2SO4 electrolyte, which displays electric double-layer capacitance with quasi-rectangular CV curves. (b) After adding redox-active K3Fe(CN)6 to the Na2SO4 electrolyte, this supercapacitor system combines two charge storage mechanisms, pseudocapacitance and electric double-layer capacitance. The novel electrode and electrolyte system can significantly increase the specific capacitance of supercapacitors.
Cu基集成电极制备过程
Fig. 9. Schematic representation of the synthesis of integrated CuO/Cu anode via chemical and electrochemical oxidation of the Cu current collector. The conversion reactions occurred within the limit of initial CuO microsheets, which include electrochemically driven nanocrystallization of CuO microsheets to CuO nanoparticles. During the discharge/charge process, the release of Cu from the current collector can maintain high capacity of CuO anode in the designed integrated anode system.
Cu基集成电极的电化学性能
Fig. 10. Electrochemical properties of CuO/Cu integrated anode. (a) Charge-discharge curves and (b) Cycling curves at current density of 100 mA g−1 and potential range of 0.01–3.0 V. Dotted line in figure indicates theoretical capacity value of CuO anode materials. (c) Rate capability curves at the current densities from 0.1 to 1.5 A g−1. (d) CV curves of CuO/Cu anode after 110 charge–discharge cycles at the scan rate of 0.1 mV/s. (e) Electrochemical impedance spectra of CuO/Cu anode. Inset shows Randle's equivalent circuit. (f) Plot of impedance phase angle versus frequency.
原位形成电极
Fig. 13. Electrochemical performance of colloidal supercapacitors. (a) The discharge and (b) charge curves measured at various current densities and potential interval of 0.8 V. (c) The specific capacitance upon current density. (d) CV curves obtained at potential range of −0.6-0.45 V and scan rate of 5 mV s−1. (e) CV curves obtained at different scan rates and potential range of −0.6–0.45 V. (f) The long-term cycling stability of MnCl2⋅4H2O colloidal supercapacitors was measured at a current density of 30 A g−1.
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读完这篇综述,是不是有种收获颇丰的感觉呀!这篇文章是由陈昆峰副研究员和薛冬峰教授撰写。
Kunfeng Chen received his BE degree of inorganic non-metallic materials engineering in 2009 and PhD of inorganic chemistry in 2014 both from Dalian University of Technology under the supervision of Prof. Dongfeng Xue. He is working as associate professor in Changchun Institute of Applied Chemistry, Chinese Academy of Sciences (CAS). His research interests focus on the controllable growth of functional materials such as graphene, metal oxide materials for electrochemical energy storage.
Professor Dongfeng Xue received his PhD from Changchun Institute of Applied Chemistry, Chinese Academy of Sciences (CIAC, CAS) in 1998. From 1999 to 2003, he worked in Universitaet Osnabrueck (AvH research fellow), University of Ottawa (Postdoc), and National Institute for Materials Science, Japan (JSPS Postdoc). In 2001, he was appointed as full professor in Dalian University of Technology. In 2011, he joined CIAC as full professor. His research interests include crystallography, crystallization, calculation and simulation of functional materials, chemical synthesis of condensed matters, and electrochemical energy storage. His scientific contributions to the community include (i) Phillips-Van Vechten-Levine-Xue bond theory, (ii) chemical bonding theory of single crystal growth, (iii) ionic electronegativity scale of 82 elements in periodic table. He has published over 400 papers in peer-reviewed journals (with h = 50), and more than 20 invited book chapters. In 2003, he was elected as corresponding member of European Academy of Sciences, Arts and Humanities (Paris). He owned visiting professorship of Queen Mary University of London (2009.1–2010.12). In 2010, he was awarded Gledden Visiting Senior Fellowship of the University of Western Australia. He also received several prestigious domestic awards, e.g., China Youth Particuology Award issued by Chinese Society of Particuology in 2010. He serves as the editorial membership of more than 20 international journals such as Materials Research Bulletin, Materials Research Innovations, Science of Advanced Materials, Journal of Porous Materials, Nanoscale Research Letters, 3D Research, Energy and Environment Focus.
最后再向大家介绍一下我们闪亮亮的JMAT期刊。它的全称是Journal of Materiomics,是由中国硅酸盐学会和Elsevier合作出版的英文期刊,现已在ScienceDirect上发布了第五卷第1期(2019年),点击文末“阅读全文“可自由获取所有论文全文。
Journal of Materiomics 为同行评议期刊,被web of science和scopus收录,cite score为8.02,从投稿到在线出版通常只需60天,并且对作者免收发表费!投稿说明详见https://www.journals.elsevier.com/journal-of-materiomics/, 期望大家不吝赐稿。